The JAK-STAT pathway controls Plasmodium vivax load in early stages of Anopheles aquasalis infection

Detalhes bibliográficos
Autor(a) principal: Bahia, Ana Cristina
Data de Publicação: 2011
Outros Autores: Kubota, Marina S., Tempone, Antônio Jorge, Araújo, Helena R. C., Guedes, Bruno A. M., Orfanó, Alessandra Silva, Tadei, Wanderli Pedro, Ríos-Velásquez, Cláudia María, Han, Yeonsoo, Secundino, Nagilá Francinete Costa, Barillas-Mury, Carolina V., Pimenta, Paulo Filemon Paolucci, Traub-Csekö, Yara Maria
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional do INPA
Texto Completo: https://repositorio.inpa.gov.br/handle/1/16170
Resumo: Malaria affects 300 million people worldwide every year and 450,000 in Brazil. In coastal areas of Brazil, the main malaria vector is Anopheles aquasalis, and Plasmodium vivax is responsible for the majority of malaria cases in the Americas. Insects possess a powerful immune system to combat infections. Three pathways control the insect immune response: Toll, IMD, and JAK-STAT. Here we analyze the immune role of the A. aquasalis JAK-STAT pathway after P. vivax infection. Three genes, the transcription factor Signal Transducers and Activators of Transcription (STAT), the regulatory Protein Inhibitors of Activated STAT (PIAS) and the Nitric Oxide Synthase enzyme (NOS) were characterized. Expression of STAT and PIAS was higher in males than females and in eggs and first instar larvae when compared to larvae and pupae. RNA levels for STAT and PIAS increased 24 and 36 hours (h) after P. vivax challenge. NOS transcription increased 36 h post infection (hpi) while this protein was already detected in some midgut epithelial cells 24 hpi. Imunocytochemistry experiments using specific antibodies showed that in non-infected insects STAT and PIAS were found mostly in the fat body, while in infected mosquitoes the proteins were found in other body tissues. The knockdown of STAT by RNAi increased the number of oocysts in the midgut of A. aquasalis. This is the first clear evidence for the involvement of a specific immune pathway in the interaction of the Brazilian malaria vector A. aquasalis with P. vivax, delineating a potential target for the future development of disease controlling strategies. © 2011 Bahia et al.
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spelling Bahia, Ana CristinaKubota, Marina S.Tempone, Antônio JorgeAraújo, Helena R. C.Guedes, Bruno A. M.Orfanó, Alessandra SilvaTadei, Wanderli PedroRíos-Velásquez, Cláudia MaríaHan, YeonsooSecundino, Nagilá Francinete CostaBarillas-Mury, Carolina V.Pimenta, Paulo Filemon PaolucciTraub-Csekö, Yara Maria2020-05-25T20:59:13Z2020-05-25T20:59:13Z2011https://repositorio.inpa.gov.br/handle/1/1617010.1371/journal.pntd.0001317Malaria affects 300 million people worldwide every year and 450,000 in Brazil. In coastal areas of Brazil, the main malaria vector is Anopheles aquasalis, and Plasmodium vivax is responsible for the majority of malaria cases in the Americas. Insects possess a powerful immune system to combat infections. Three pathways control the insect immune response: Toll, IMD, and JAK-STAT. Here we analyze the immune role of the A. aquasalis JAK-STAT pathway after P. vivax infection. Three genes, the transcription factor Signal Transducers and Activators of Transcription (STAT), the regulatory Protein Inhibitors of Activated STAT (PIAS) and the Nitric Oxide Synthase enzyme (NOS) were characterized. Expression of STAT and PIAS was higher in males than females and in eggs and first instar larvae when compared to larvae and pupae. RNA levels for STAT and PIAS increased 24 and 36 hours (h) after P. vivax challenge. NOS transcription increased 36 h post infection (hpi) while this protein was already detected in some midgut epithelial cells 24 hpi. Imunocytochemistry experiments using specific antibodies showed that in non-infected insects STAT and PIAS were found mostly in the fat body, while in infected mosquitoes the proteins were found in other body tissues. The knockdown of STAT by RNAi increased the number of oocysts in the midgut of A. aquasalis. This is the first clear evidence for the involvement of a specific immune pathway in the interaction of the Brazilian malaria vector A. aquasalis with P. vivax, delineating a potential target for the future development of disease controlling strategies. © 2011 Bahia et al.Volume 5, Número 11Attribution-NonCommercial-NoDerivs 3.0 Brazilhttp://creativecommons.org/licenses/by-nc-nd/3.0/br/info:eu-repo/semantics/openAccessJanus KinaseNitric Oxide SynthaseProtein Inhibitor Of Activated StatStat ProteinNitric Oxide SynthaseProtein Inhibitor Of Activated StatStat ProteinAnophelesAnopheles AquasalisControlled StudyEpithelium CellFemaleGeneGene SequenceGene SilencingHumanImmunityImmunocytochemistryMalariaMaleNonhumanNos GeneNucleotide SequenceOocystOrganismal InteractionParasite LoadPias GenePlasmodium VivaxProtein ExpressionProtozoal GeneticsRna InterferenceStat GeneAnimalsAnophelesBiosynthesisBrasilDna SequenceGene Expression ProfilingImmunohistochemistryImmunologyIsolation And PurificationMolecular GeneticsParasitologyAnimalAnophelesBrasilFemaleGene Expression ProfilingGene Knockdown TechniquesImmunohistochemistryMaleMolecular Sequence DataNitric Oxide SynthasePlasmodium VivaxProtein Inhibitors Of Activated StatSequence Analysis, DnaStat Transcription FactorsThe JAK-STAT pathway controls Plasmodium vivax load in early stages of Anopheles aquasalis infectioninfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlePLoS Neglected Tropical Diseasesengreponame:Repositório Institucional do INPAinstname:Instituto Nacional de Pesquisas da Amazônia (INPA)instacron:INPAORIGINALJAK-STAT.pdfJAK-STAT.pdfapplication/pdf1179975https://repositorio.inpa.gov.br/bitstream/1/16170/1/JAK-STAT.pdf15ee0db2d9d480410238841f95816d08MD511/161702020-07-14 11:27:24.972oai:repositorio:1/16170Repositório de PublicaçõesPUBhttps://repositorio.inpa.gov.br/oai/requestopendoar:2020-07-14T15:27:24Repositório Institucional do INPA - Instituto Nacional de Pesquisas da Amazônia (INPA)false
dc.title.en.fl_str_mv The JAK-STAT pathway controls Plasmodium vivax load in early stages of Anopheles aquasalis infection
title The JAK-STAT pathway controls Plasmodium vivax load in early stages of Anopheles aquasalis infection
spellingShingle The JAK-STAT pathway controls Plasmodium vivax load in early stages of Anopheles aquasalis infection
Bahia, Ana Cristina
Janus Kinase
Nitric Oxide Synthase
Protein Inhibitor Of Activated Stat
Stat Protein
Nitric Oxide Synthase
Protein Inhibitor Of Activated Stat
Stat Protein
Anopheles
Anopheles Aquasalis
Controlled Study
Epithelium Cell
Female
Gene
Gene Sequence
Gene Silencing
Human
Immunity
Immunocytochemistry
Malaria
Male
Nonhuman
Nos Gene
Nucleotide Sequence
Oocyst
Organismal Interaction
Parasite Load
Pias Gene
Plasmodium Vivax
Protein Expression
Protozoal Genetics
Rna Interference
Stat Gene
Animals
Anopheles
Biosynthesis
Brasil
Dna Sequence
Gene Expression Profiling
Immunohistochemistry
Immunology
Isolation And Purification
Molecular Genetics
Parasitology
Animal
Anopheles
Brasil
Female
Gene Expression Profiling
Gene Knockdown Techniques
Immunohistochemistry
Male
Molecular Sequence Data
Nitric Oxide Synthase
Plasmodium Vivax
Protein Inhibitors Of Activated Stat
Sequence Analysis, Dna
Stat Transcription Factors
title_short The JAK-STAT pathway controls Plasmodium vivax load in early stages of Anopheles aquasalis infection
title_full The JAK-STAT pathway controls Plasmodium vivax load in early stages of Anopheles aquasalis infection
title_fullStr The JAK-STAT pathway controls Plasmodium vivax load in early stages of Anopheles aquasalis infection
title_full_unstemmed The JAK-STAT pathway controls Plasmodium vivax load in early stages of Anopheles aquasalis infection
title_sort The JAK-STAT pathway controls Plasmodium vivax load in early stages of Anopheles aquasalis infection
author Bahia, Ana Cristina
author_facet Bahia, Ana Cristina
Kubota, Marina S.
Tempone, Antônio Jorge
Araújo, Helena R. C.
Guedes, Bruno A. M.
Orfanó, Alessandra Silva
Tadei, Wanderli Pedro
Ríos-Velásquez, Cláudia María
Han, Yeonsoo
Secundino, Nagilá Francinete Costa
Barillas-Mury, Carolina V.
Pimenta, Paulo Filemon Paolucci
Traub-Csekö, Yara Maria
author_role author
author2 Kubota, Marina S.
Tempone, Antônio Jorge
Araújo, Helena R. C.
Guedes, Bruno A. M.
Orfanó, Alessandra Silva
Tadei, Wanderli Pedro
Ríos-Velásquez, Cláudia María
Han, Yeonsoo
Secundino, Nagilá Francinete Costa
Barillas-Mury, Carolina V.
Pimenta, Paulo Filemon Paolucci
Traub-Csekö, Yara Maria
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Bahia, Ana Cristina
Kubota, Marina S.
Tempone, Antônio Jorge
Araújo, Helena R. C.
Guedes, Bruno A. M.
Orfanó, Alessandra Silva
Tadei, Wanderli Pedro
Ríos-Velásquez, Cláudia María
Han, Yeonsoo
Secundino, Nagilá Francinete Costa
Barillas-Mury, Carolina V.
Pimenta, Paulo Filemon Paolucci
Traub-Csekö, Yara Maria
dc.subject.eng.fl_str_mv Janus Kinase
Nitric Oxide Synthase
Protein Inhibitor Of Activated Stat
Stat Protein
Nitric Oxide Synthase
Protein Inhibitor Of Activated Stat
Stat Protein
Anopheles
Anopheles Aquasalis
Controlled Study
Epithelium Cell
Female
Gene
Gene Sequence
Gene Silencing
Human
Immunity
Immunocytochemistry
Malaria
Male
Nonhuman
Nos Gene
Nucleotide Sequence
Oocyst
Organismal Interaction
Parasite Load
Pias Gene
Plasmodium Vivax
Protein Expression
Protozoal Genetics
Rna Interference
Stat Gene
Animals
Anopheles
Biosynthesis
Brasil
Dna Sequence
Gene Expression Profiling
Immunohistochemistry
Immunology
Isolation And Purification
Molecular Genetics
Parasitology
Animal
Anopheles
Brasil
Female
Gene Expression Profiling
Gene Knockdown Techniques
Immunohistochemistry
Male
Molecular Sequence Data
Nitric Oxide Synthase
Plasmodium Vivax
Protein Inhibitors Of Activated Stat
Sequence Analysis, Dna
Stat Transcription Factors
topic Janus Kinase
Nitric Oxide Synthase
Protein Inhibitor Of Activated Stat
Stat Protein
Nitric Oxide Synthase
Protein Inhibitor Of Activated Stat
Stat Protein
Anopheles
Anopheles Aquasalis
Controlled Study
Epithelium Cell
Female
Gene
Gene Sequence
Gene Silencing
Human
Immunity
Immunocytochemistry
Malaria
Male
Nonhuman
Nos Gene
Nucleotide Sequence
Oocyst
Organismal Interaction
Parasite Load
Pias Gene
Plasmodium Vivax
Protein Expression
Protozoal Genetics
Rna Interference
Stat Gene
Animals
Anopheles
Biosynthesis
Brasil
Dna Sequence
Gene Expression Profiling
Immunohistochemistry
Immunology
Isolation And Purification
Molecular Genetics
Parasitology
Animal
Anopheles
Brasil
Female
Gene Expression Profiling
Gene Knockdown Techniques
Immunohistochemistry
Male
Molecular Sequence Data
Nitric Oxide Synthase
Plasmodium Vivax
Protein Inhibitors Of Activated Stat
Sequence Analysis, Dna
Stat Transcription Factors
description Malaria affects 300 million people worldwide every year and 450,000 in Brazil. In coastal areas of Brazil, the main malaria vector is Anopheles aquasalis, and Plasmodium vivax is responsible for the majority of malaria cases in the Americas. Insects possess a powerful immune system to combat infections. Three pathways control the insect immune response: Toll, IMD, and JAK-STAT. Here we analyze the immune role of the A. aquasalis JAK-STAT pathway after P. vivax infection. Three genes, the transcription factor Signal Transducers and Activators of Transcription (STAT), the regulatory Protein Inhibitors of Activated STAT (PIAS) and the Nitric Oxide Synthase enzyme (NOS) were characterized. Expression of STAT and PIAS was higher in males than females and in eggs and first instar larvae when compared to larvae and pupae. RNA levels for STAT and PIAS increased 24 and 36 hours (h) after P. vivax challenge. NOS transcription increased 36 h post infection (hpi) while this protein was already detected in some midgut epithelial cells 24 hpi. Imunocytochemistry experiments using specific antibodies showed that in non-infected insects STAT and PIAS were found mostly in the fat body, while in infected mosquitoes the proteins were found in other body tissues. The knockdown of STAT by RNAi increased the number of oocysts in the midgut of A. aquasalis. This is the first clear evidence for the involvement of a specific immune pathway in the interaction of the Brazilian malaria vector A. aquasalis with P. vivax, delineating a potential target for the future development of disease controlling strategies. © 2011 Bahia et al.
publishDate 2011
dc.date.issued.fl_str_mv 2011
dc.date.accessioned.fl_str_mv 2020-05-25T20:59:13Z
dc.date.available.fl_str_mv 2020-05-25T20:59:13Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://repositorio.inpa.gov.br/handle/1/16170
dc.identifier.doi.none.fl_str_mv 10.1371/journal.pntd.0001317
url https://repositorio.inpa.gov.br/handle/1/16170
identifier_str_mv 10.1371/journal.pntd.0001317
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Volume 5, Número 11
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivs 3.0 Brazil
http://creativecommons.org/licenses/by-nc-nd/3.0/br/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivs 3.0 Brazil
http://creativecommons.org/licenses/by-nc-nd/3.0/br/
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv PLoS Neglected Tropical Diseases
publisher.none.fl_str_mv PLoS Neglected Tropical Diseases
dc.source.none.fl_str_mv reponame:Repositório Institucional do INPA
instname:Instituto Nacional de Pesquisas da Amazônia (INPA)
instacron:INPA
instname_str Instituto Nacional de Pesquisas da Amazônia (INPA)
instacron_str INPA
institution INPA
reponame_str Repositório Institucional do INPA
collection Repositório Institucional do INPA
bitstream.url.fl_str_mv https://repositorio.inpa.gov.br/bitstream/1/16170/1/JAK-STAT.pdf
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bitstream.checksumAlgorithm.fl_str_mv MD5
repository.name.fl_str_mv Repositório Institucional do INPA - Instituto Nacional de Pesquisas da Amazônia (INPA)
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